首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >An ultrasensitive conformation-dependent colorimetric probe for the detection of mercury(II) using exonuclease III-assisted target recycling and gold nanoparticles
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An ultrasensitive conformation-dependent colorimetric probe for the detection of mercury(II) using exonuclease III-assisted target recycling and gold nanoparticles

机译:使用外切核酸酶III辅助靶再循环和金纳米颗粒检测用于检测汞(II)的超敏化构象依赖性比色探针

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摘要

An ultrasensitive conformation-dependent colorimetric assay has been developed for the detection of mercury(II) ions. It is based on the use of exonuclease III (Exo III)-assisted target recycling and gold nanoparticles (AuNPs). In the absence of Hg(II), the hairpin-shaped DNA probe (H-DNA) binds to AuNPs and stabilizes them in solutions of high ionic strength. In the presence of Hg(II), on the other hand, the sticky termini of the H-DNA form a rigid DNA duplex stem with a blunt 3'-terminus. Thus, Exo III is activated as a biocatalyst for selective and stepwise removal of mononucleotides from the 3'-terminus of the H-DNA. As a result, Hg(II) is released from the T-Hg(II)-T complexes. The guanine-rich sequences released from the H-DNA are then self-assembled with potassium ion to form a stable G-quadruplex conformation. In solutions of high ionic strength, this results in aggregation of AuNPs and a color change from red to blue which can be seen with bare eyes. The method is highly sensitive and selective. It has a linear response in the 10 pM to 100 nM Hg(II) concentration range, and the detection limit is as low as 3.2 pM (at an S/N ratio of 3). The relative standard deviation at a level of 0.5 nM of Hg(II) is 4.9% (for n = 10). The method was applied to the detection of Hg(II) in spiked environment water samples, with recoveries ranging from 92% to 106%.
机译:已经开发出超细构象依赖性比色测定用于检测汞(II)离子。它是基于外切核酸酶III(EXO III)的目标回收和金纳米颗粒(AUNP)的使用。在没有Hg(II)的情况下,发夹形DNA探针(H-DNA)与AUNP结合并稳定在高离子强度的溶液中。另一方面,在Hg(ii)的存在下,H-DNA的粘性末端形成刚性DNA双链茎,其具有钝的3'-末端。因此,EXO III被激活为生物催化剂,用于选择性和逐步从H-DNA的3'-末端去除单核苷酸。结果,Hg(II)从T-Hg(II)络合物中释放。然后将从H-DNA释放的富含致氢的序列用钾离子自组装以形成稳定的G-Quadreplex构象。在高离子强度的解决方案中,这导致AUNP的聚集和从红色到蓝色的颜色变化,这可以用裸眼睛看到。该方法具有高度敏感和选择性。它在10PP至100nm Hg(II)浓度范围内具有线性响应,并且检测极限低至3.2μm(以S / N比为3)。 Hg(II)的0.5nm水平的相对标准偏差为4.9%(对于n = 10)。将该方法应用于尖刺环境水样中HG(II)的检测,回收率范围为92%至106%。

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